Functional sheet with protective films

Abstract

A functional sheet with protective films obtained by laminating protective sheets includes aromatic polycarbonate onto a functional layer that is a polyvinyl alcohol polarizing layer or a photocromic layer or any combination thereof and having the protective films adhere to the protective sheets. The protective films have at least two or three layers i.e., a base layer composed of a polypropylene that has a melting point higher than the glass transition temperature of an aromatic polycarbonate; an adhesive layer composed of a heat plastic polyolefin elastomer composed of a polyolefin that has a melting point from a temperature that is 15 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature that is lower than the glass transition temperature and a styrene-olefin-styrene co-poly-elastomer; and a middle layer composed of a polyolefin resin between the base layer and the adhesive layer.

Claims

1. A functional sheet with protective films obtained by laminating protective sheets comprised of aromatic polycarbonate onto a functional layer that is a polyvinyl alcohol polarizing layer or a photocromic layer or any combination thereof and having the protective films adhere to the protective sheets, wherein the protective films have at least two layers, i.e., a base layer that is composed of a polypropylene that has a melting point higher than the glass transition temperature of an aromatic polycarbonate and an adhesive layer that is a resin composition that comprises a polyolefin that has a melting point from a temperature that is 15 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature that is lower than the glass transition temperature and a styrene-olefin-styrene co-poly-elastomer.

2. The functional sheet with protective films of claim 1, wherein the polypropylene that is used for the base layer is a low density polypropylene and its melting point is 150-170 C. and the thickness of the base layer is 30-60 m.

3. The functional sheet with protective films of claim 1, wherein the polyolefin of the adhesive layer is a low density polyolefin and the melting point of the polyolefin is 135-145 C. and the thickness of the adhesive layer is 5-30 m.

4. The functional sheet with protective films of claim 1, wherein the protective film has a layer composed of a polyolefin resin between the base layer and the adhesive layer and the melting point of the layer composed of the polyolefin resin is lower than that of the base layer.

5. The functional sheet with protective films of claim 4, wherein the layer composed of the polyolefin resin is a low density polyolefin and the melting point of the layer is 120-145 C., and the layer is 20-60 m thick.

6. A method for producing polycarbonate injection molded lens comprising these steps: laminating protective sheets comprised of aromatic polycarbonate onto a functional layer that is a polyvinyl alcohol polarizing layer or a photochromic layer or any combination thereof and having protective films adhere onto the protective sheets to obtain a functional sheet with protective films; punching the functional sheet to form a shape of interest; heat-curving the punched functional sheet and setting the sheet on a mold for injection molding after removing the protective films; injecting the [molten] aromatic polycarbonate resin; and recovering a molded product, wherein the protective films have at least two layers, i.e., a base layer that is composed of a polypropylene that has a melting point higher than the glass transition temperature of an aromatic polycarbonate and an adhesive layer that is a resin composition that comprises a polyolefin that has a melting point from a temperature that is 15 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature that is lower than the glass transition temperature and a styrene-olefin-styrene co-poly-elastomer.

7. The method for producing polycarbonate injection molded lens of claim 6, wherein the heat-curving is carried out by slow deformation at a temperature that is 15-5 C. lower than the temperature of the glass transition temperature of an aromatic polycarbonate.

8. The method for producing polycarbonate injection molded lens of claim 6, wherein the polypropylene that is used for the base layer is a low density polypropylene and its melting point is 150-170 C. and the base layer is 30-60 m thick.

9. The method for producing polycarbonate injection molded lens of claim 6, wherein the polyolefin of the adhesive layer is a low density polyolefin and its melting point is 135-145 C. and the adhesive layer is 5-30 m thick.

10. The method for producing polycarbonate injection molded lens of claim 6, wherein the protective film has a layer composed of a polyolefin resin between the base layer and the adhesive layer and the melting point of the polyolefin resin is lower than that of the base layer.

11. The method for producing polycarbonate injection molded lens of claim 6, wherein the layer composed of a polyolefin resin is a low density polyolefin and the melting point of the polyolefin resin is 120-145 C., and the layer that is composed of a polyolefin resin is 20-60 m thick.

Description

BRIEF EXPLANATIONS OF FIGURES

(1) FIGS. 1-A and 1-B disclose photos that show sections of the heat-curving products obtained by punching the functional sheet with the protective sheet of the present invention and subjecting the punched sheet to the heat-curving process. FIG. 1-A shows a functional sheet with the protective films of Comparative example 1. FIG. 1-B shows the functional sheet with the protective films of Example 1.

EMBODIMENTS TO CARRY OUT THE INVENTION

Protective Films

(2) The protective film of the present invention is composed of at least two layers. One is a base layer and the other is an adhesive layer. Alternatively, the film is composed of three layers where an additional middle layer is located between the base layer and the adhesive layer. The thickness of the protective films of the present invention can be selected within the scope of 50-100 m.

(3) The main role of the base layer of the protective film is protecting the surface of the functional sheet from flaws, stains, or contaminants that may exist during the handling of the commercial distribution or various processing steps. This is the fundamental function of the protective film. The layer should be composed of a film that has the appropriate film strength. Further, during the punching process the resins to be used for the base layer do not make any cracks that will become small pieces and do not separate from the adhesive layer. Further, they do not melt or adhere to the contacting layers when they are exposed to a temperature around the glass transition temperature of an aromatic polycarbonate in the heat-curving process. The resins maintain an [initial] adhered state with a molten adhesive layer.

(4) Further, when many functional sheets with protective sheets are stacked and stored for a long time, the surfaces of the protective films are pressed and contacted during this storage. At this time, to prevent blocking, where the stacked surfaces cannot be separated, generally making an additional hard surface on the base layer of the protective film, applying an anti-stacking agent on the surface, etc., are done accordingly.

(5) The base layer does not melt during the heat-curving process. The base layer is selected from polypropylenes that have a melting point higher than the glass transition temperature of an aromatic polycarbonate (a peak temperature measured by a DSC measurement). Preferably, the melting point is 150-170 C., more preferably 155-165 C. Preferably, the polycarbonate is selected from low density polypropylenes. The base layer is selected to be from 20 to 60 m thick. High-density polypropylenes are brittle [against the stress of the punching process] and therefore residues from the punching process can be easily produced. [In contrast] polypropylenes that have low melting points bring about problems caused by their low stress strength. Thus, [in the punching process] they cannot maintain their shapes.

(6) The protective films of the present invention may not show clear peaks in a thermal measurement. Especially, the resins to be used in the adhesive layer have densities lower than the resin of the base materials, and are very thin. Thus, generally they show low and gentle sloping peaks. Further, in the present invention, the adhesive layer is a composition of a polyolefin and a polyolefin rubber. Thus, the starting parts of the peak of the melting point of the base layer should be carefully distinguished from those of the peak of the adhesive layer.

(7) The adhesive layer (or a temporary adhesive layer) maintains an adhesiveness to the base layer or the middle layer. Further, it has to adhere to the surfaces of the aromatic polycarbonate. When the adhesive layer is separated, no glue remains on the surface of the functional sheet. As explained above, the adhesive layer has an adhesiveness where the base layer [of the protective film] does not separate from the surface of the aromatic polycarbonate or from the base layer during the punching process. Further, the adhesive layer maintains its adhesiveness, even if it is in a molten state. An adhesive layer that has a small dependency of viscosity at a melting point and a layer that shows unclear melting points, such as low-density resins with irregular structures, or with branching structures, are exemplary resins to be used as the adhesive layer of the present invention.

(8) The adhesive layer has a melting point between a temperature that is 15 C. lower than the glass transition temperature of the aromatic polycarbonate and a temperature that is less than the glass transition temperature. The preferable melting point of the polyolefin to be used for the adhesive layer is 135-145 C. The adhesive layer is a resin composition of a low-density polyolefin and an elastomer comprised of styrene-olefin-styrene block co-poly-elastomer. The thickness of the adhesive layer is not limited. However, it is generally from 5-30 m.

(9) When the polyolefin of the adhesive layer is pressed to have it adhere to the aromatic polycarbonate at room temperature, it has not enough adhesiveness to do so. When a polyolefin that has a low melting point is used alone in the adhesive layer, a strong adhesiveness is produced. Such an adhesiveness is reinforced when the adhesive layer is subjected to the heat-curving process. Then it is cooled to room temperature, but the reduction of the reinforced adhesiveness is not enough. Thus, such a polyolefin is not preferable. In contrast, if the polyolefin to be used for the adhesive layer has a high melting point, then to obtain the adhesiveness of interest more styrene-olefin-styrene copolymerized elastomer is needed. In such a case, a weak adhesiveness of the adhesive layer to the base layer is a problem. In another embodiment, if the melting point is too high, a weak adhesiveness of the adhesion layer to the middle layer is a problem.

(10) A styrene-olefin-styrene copolymerized elastomer is denoted SBS, SIS, etc. Specifically, it is an elastomeric copolymer that is comprised of chains of polyolefins, such as an ethylene-butene copolymer, an ethylene-pentene copolymer, etc. Such polyolefin chains are obtained by hydrogenation of unsaturated double bonds of a thermoplastic elastomer, such as polybutadiene of a styrene-butadiene-styrene block copolymer and such as polyisoprene of a styrene-isoprene-styrene copolymer.

(11) At room temperature the polystyrene chains at both ends of the polymer appear to be associated with other polystyrene chains in a state of microparticles, to thereby make structures of the pseudo-bridges of the elastomeric polyolefin chains. At room temperature, the elastomer behaves like cross-linked rubbers. At temperatures higher than the melting points of polystyrene, they are easily melted and flow.

(12) The ratio of the components of the elastomer is selected so that the elastomeric polyolefin chains are 20-60%, preferably 28-52%, of the resin composition [of the adhesive layer].

(13) In an adhesion (or a temporary adhesion), there is a problem that relates to a change of the adhesiveness by aging. For the purpose of the present invention, elastomers that do not show such a change are preferable. For example, in the change of the adhesiveness by aging, generally the adhesiveness (or gluing) unnecessarily increases. Therefore blocking, i.e., a state where stacked functional sheets cannot be separated, occurs. Such stacked functional sheets become unusable. The adhesiveness of the protective films of the functional sheet of the present invention shows a value for the adhesiveness that is less than that of a conventional adhesive agent. Thus, in the present invention such a problem would not arise. However, to carry out the present invention the change of the adhesiveness by aging should be considered.

(14) The protective films of the present invention essentially have two layers. One is a base layer and the other is an adhesive layer (or a temporary gluing layer). They can have a middle layer or a support layer between the base layer and the adhesive layer (or a temporary gluing layer) or the inside of the base layer. The support layer or the middle layer is composed of polyolefin resins that have melting points lower than the melting point of the base layer.

(15) The polyolefin resins that form the middle layer comprise polyolefins that have a melting point that is 40 C. less than the glass transition temperature of an aromatic polycarbonate, to 5 C. less than that. A preferable melting point is from 120 C. to 145 C. The middle layer is 20-60 m thick. The middle layer becomes molten in the heat-curving process, and therefore it absorbs a local stress loading. Further, since the middle layer is sandwiched by the base layer and the adhesive layer and held there, even if it becomes molten it does not move out of the protective film.

(16) When the melting point of the polyolefin of the middle layer is about 120 C., the layer should be about 20 m thick to prevent the separation of it from the protective film itself. Further, when the melting point of the polyolefin of the middle layer is about 140 C., the layer should be about 40 m thick, to increase the effect to absorb the stress loading. However, the melting point and the thickness of the middle layer should be based on the conditions of the heat-curving process and the working environment.

(17) When the melting point of the middle layer is higher than that within the scope of the melting points disclosed above, since in the heat-curving process of a punched functional sheet the middle layer melts but does not flow, it does not absorb sufficient stress loading. Therefore the problems of wrinkles when the protective film is removed, unevenness of the surface, and the flames, are not resolved. When the melting point of the middle layer is lower than that within the scope of the melting point disclosed above, the melted middle layer that occurs during at the heat-curving process flows by the stress of the decompression or the pressure of the heat-curving process, and then the flowing middle layer becomes a projection that overhangs the base layer and the adhesive layer. The projection adheres to the section of the heat-curving products or becomes separate pieces on the section. When such a heat-curving product is used for the injection molding process after the protective films are removed, the white streaks would arise. This is not preferable.

(18) The protective film of the present invention is generally produced by the coextrusion.

(19) The protective films are produced by using at least two extruders, one for the base layer (a core layer) and one for the adhesive layer (or a gluing layer). Alternatively, they are produced by using three extruders, to include one additional extruder, for the middle layer. In each extruder, resins for each layer are melted and extruded. Then in a co-extruding die the molten and extruded resins contact each other to make a laminate. The laminate is pressed out from a die lip and drawn by using a roll to make the protective films. In this co-extrusion, a small amount of additives, such as a stabilizer, a remover, and a slip agent, can be added to carry out a uniform extrusion and to prevent adhesions of the resins to the roll.

(20) Functional Sheet

(21) The protective films disclosed above protect the surfaces of the functional sheet by adhesion of the protective films to the surfaces of the functional sheet. The functional sheet is a laminate where a functional layer that is selected from a polyvinyl alcohol polarizing film layer, a photochromic layer, or combinations thereof, is sandwiched with the aromatic polycarbonate sheets or films.

(22) The functional film of the polyvinyl alcohol polarizing film layer is generally produced by uniaxially stretching of a polyvinyl alcohol film in an aqueous solution and adsorbing and aligning dichroic organic dyes. It is stretched to 3.5-6.5 times its original length and is treated by boric acid and metal compounds.

(23) The photochromic layer is a layer obtained by mixing photochromic compounds (photocromic materials) with transparent resins. The photocromic materials to be used are spirooxazine-based materials, spiropyran-based materials, fulgide-based materials, diarylethene-based materials, and salicylideneaniline-based materials.

(24) The aromatic polycarbonate sheet or film is 0.1-1 mm thick, preferably 0.2-0.5 mm thick. The retardation after the uniaxial orientation is 2,000 nm or more. Generally, 10,000 nm or less of the retardation is preferable.

(25) The aromatic polycarbonate resin used is polymers produced according to the well-known method from a bisphenol compound typified by 2,2-bis(4-hydroxyphenyl)alkane or 2,2-(4-hydroxy-3,5-dihalogenophenyl)alkane. The polymer skeleton thereof may include a structural unit derived from a fatty acid diol or a structural unit having ester bonds. In particular, an aromatic polycarbonate produced from 2,2-bis(4-hydroxyphenyl)propane is preferred. Regarding the molecular weight of the aromatic polycarbonate, for the ability to be formed and the mechanical strength the viscosity-average molecular weight is preferably 7,000 to 40,000, and the viscosity-average molecular weight is particularly preferable when it is 20,000 to 34,000.

(26) The functional sheet of the present invention is produced by laminating the functional layer explained above between the aromatic polycarbonate sheets or films. This lamination is carried out by laminating the aromatic polycarbonate sheets to each side of the functional films by means of an adhesive layer, and crimping them. If needed, the adhesive layer is set (cured).

(27) Another embodiment, where a polyvinyl alcohol polarizing film is used as the functional film, is carried out by continuously applying and drying the adhesive agent on one side of the long polyvinyl alcohol polarizing film, putting and crimping the aromatic polycarbonate sheet on the side where the adhesive agent was continuously applied, and drying the adhesive agent on the other side of the long polyvinyl alcohol polarizing film, and putting and crimping the aromatic polycarbonate sheet on the side that has had applied the adhesive agent. Then the obtained laminate sheet comprised of the aromatic polycarbonate sheets and the functional layer is wound around a roller or is cut to have the size of interest, and cured.

(28) The Functional Sheet with the Protective Films

(29) The functional sheet with the protective films of the present invention is generally obtained by laminating the protective film, which is a continuous film, on both sides of the functional sheet, which is a continuous sheet, or a cut sheet, and crimping the films to the sheet. Crimping is generally carried out by passing the laminate body through between two rollers. It is carried out under the conditions of 10 kg/cm of pressure and 60-80 C., the temperature of the surface of the two rollers. Further, the method for laminating the protective films of the present invention is not limited to that explained above. As long as laminates have the same structures as the laminate obtained by this method, any method can be used.

(30) Injection Molded Lends

(31) Further, the present invention relates to a method for producing a polycarbonate injection molded lens. The method comprises of the steps of: laminating protective sheets comprised of aromatic polycarbonate onto a functional layer that is a polyvinyl alcohol polarizing layer or a photochromic layer or any combinations thereof and adhering the protective films to the protective sheets; punching the functional sheet to form a shape of interest; heat-curving the punched sheet, setting the sheet on a mold for injection molding after removing the protective films; injecting the [molten] aromatic polycarbonate resin; and recovering a molded product.

(32) The protective films have at least two layers, i.e., a base layer that is composed of polypropylene that has a melting point higher than the glass transition temperature of an aromatic polycarbonate and an adhesive layer that is composed of a heat plastic polyolefin elastomer [composition] that is composed of a polyolefin that has a melting point of a temperature that is 15 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature that is lower than the glass transition temperature and polyolefin rubbers.

(33) Further, the heat-curving is carried out by a slow deformation at a temperature that is at most 15-5 C. lower than the temperature of the glass transition temperature of an aromatic polycarbonate.

(34) Another embodiment of the present invention is the method for producing polycarbonate injection molded lens where the protective films have at least three layers, i.e., the base layer, which has a melting point higher than the glass transition temperature of the aromatic polycarbonate, the adhesive layer, which is comprised of a composition of a polyolefin and a styrene-olefin-styrene copolymeric elastomer, where the polyolefin has a melting point of a temperature that is 15 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature that is less than the glass transition temperature of the aromatic polycarbonate, and a middle layer, which is between the base layer and the adhesive layer and that has a melting point between a temperature that is 40 C. higher than the glass transition temperature of the aromatic polycarbonate and a temperature that is less than the glass transition temperature.

(35) The functional sheet with the protective films of the present invention is subject to the punching process to cut it to form the shape of interest. For example, it can be a disk that has an 80 mm diameter or a slit shape that is cut perpendicularly in the same width at both ends. On a punching machine that has the blade of interest, e.g., Thomson blades, taking directions, etc., of the functional sheet with the protective films of the present invention and a backing plate, into consideration, they are stacked. Then the functional sheet is cut.

(36) The cut pieces are subjected to the heat-curving process that uses the mold of interest, generally a mold that has a partially spherical body. The preheating of the pieces is carried out at a temperature that is 15-5 C. lower than the glass transition temperature of the aromatic polycarbonate. Preferably, the pieces are preheated to 130 C. or more. The cut pieces are set in a preheated female-type die. Then the pieces are gradually deformed at a temperature that is at most 15-5 C. lower than the glass transition temperature of the aromatic polycarbonate, generally at 135-145 C. The deformation generally takes 0.5-10 minutes. During the deformation, a male-type die is used accordingly.

(37) By the temperature of the heat-curving process, the adhesive layer of the protective film of the present invention appears to be partially melted. However, it does not adhere to the cut section, and unlike the conventional protective film, therefore no white streak is produced.

(38) The polyolefin used for the adhesive layer of the protective film has a melting point that is within the scope of the highest temperature of the heat-curving process. However, when the polyolefin is blended to make a composition to be used for the adhesive layer, the melting point of the polyolefin appears to be unclear or difficult to distinguish from the peaks of the other components of the composition. The adhesive layer of the conventional protective film shows clear peaks. A comparison of the peaks of the adhesive layer of the conventional protective film with those of the adhesive layer of the protective film of the present invention shows that the peaks of the adhesive layer of the present invention are unclear and are higher than the peaks of the adhesive layer of the conventional one.

(39) The adhesive layer of the protective film of the present invention has a high viscosity. Thus, when it is subjected to the heat-curving process it does not flow, nor is it removed from the base layer. Further, it does not produce a molten part that adheres to the cut section of the functional sheet.

(40) The protective films attached to the cut piece after the heat-curving process are removed. Then the piece is set on a mold of an injection molding machine and heated to the temperature of interest. Then an optical aromatic polycarbonate resin material is injected onto the cut piece to produce an aromatic polycarbonate injection molded lens.

(41) The injection molding of the present invention is carried out by using the resin that is heated to 260-340 C., preferably to 270-310 C. The pressure to be used for the injection molding is 50-200 MPa, preferably 80-150 MPa. The temperature of the mold is 60-130 C., preferably 80-125 C.

(42) The aromatic polycarbonate injection molded lens obtained by the steps explained above is subjected to a treatment to make a hard coat. It is further subjected to a treatment to make a mirror coat and an anti-reflective coat. Then finished products are obtained.

(43) Preferable materials and conditions for the finished processes should be chosen based on the appearance of interest of the finished products, adhesiveness to the inorganic substances used for the mirror coat, anti-reflective coat, etc. From this point, the temperature of the calcination of the finished products is preferably a temperature from 50 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature less than the glass transition temperature. Preferably, the temperature of the calcination is a temperature from 40 C. lower than the glass transition temperature of the aromatic polycarbonate to a temperature 15 C. lower than the glass transition temperature. Preferably, it is about 120 C. The time to make the hard coat treatment is about 0.5-2 hours. Below the exemplary embodiments of the present invention are explained.

(44) Functional Sheet

(45) On both surfaces of a polarizing film that is 30 m thick, aromatic polycarbonate sheets that are 0.3 mm thick are laminated by using thermosetting polyurethane-based adhesive layers to construct a functional sheet that is 0.6 mm thick, 300 mm wide, and 340 mm long (Mitsubishi Gas Chemical Co., Inc., Iupilonpola). On both surfaces of the functional sheet the protective films disclosed in Table 1 are crimped (at 10 kg/cm of loading) by using heated rollers (the temperature of the surface of each roller is 73 C.) (Examples 1 and 2 and Comparative examples 1-4).

(46) On both surfaces of a polarizing film that is 30 m thick, aromatic polycarbonate sheets that are 0.3 mm thick are laminated by using thermosetting polyurethane-based adhesive layers to construct a functional sheet 0.6 mm thick, 300 mm wide, and 340 mm long (Mitsubishi Gas Chemical Co., Inc., Iupilonpola). On both surfaces of the functional sheet, the protective films disclosed in Table 3 are crimped (at 10 kg/cm of loading) by using heated rollers (the temperature of the surface of each roller is 80 C.) (Examples 3, 4, and 5 and Comparative examples 5 and 6).

(47) Next, the obtained functional sheets with the protective sheets are subjected to the punching process.

(48) By the conventional methods the press punching process that uses Thomson blades is used. As explained in the section on the problem to be solved of the present invention, in this example the high frequency of the white streaks are necessary [to estimate the effect of the protective films in the present invention]. Thus, single-edged Thomson blades are used. The edges of the blades are set so that they face outwards. Further, five m (micro meters) of the tops of the edges were cut off.

(49) Shape of the Cut Piece

(50) The shape of the punched piece of the functional sheet with the protective films is a vertical section, such as a slit shape, a capsule, or a straw rice bag, where both sides of the line that passes through the center of a disc, whose diameter is 80 mm, are cut perpendicularly in the same width, 55 mm. Both sides that are not parallel have small projections on an arc of each side. The projections are used for positioning in a mold for heat-curving process. The long direction of the cut piece is parallel to the direction of the absorption axis of the polarizing film.

(51) The cut piece produced by the procedures explained above was subjected to the heat-curving process. In this process, the cut piece was preheated in a pre-heater. Then it was transferred to a partially spherical female die that has the curvature of interest and pressed by using a male die made of silicon rubbers. At the same time, it was absorbed by the female die by using decompression, and the male die was raised upward. The piece adsorbed onto the female die was held for the time of interest at the temperature generated by the hot air circulation. After that, the piece was recovered. These steps were carried out in a continuous heat-curving machine.

(52) In these steps, the piece was preheated in the pre-heater where an atmosphere in the heater is maintained at 136 C. The partial spherical curvature of the female die is about 8R (about a radius of 65.6 mm). The temperature of the surface of the female die is 138 C. The time to press by the male die is 4 seconds. The piece was absorbed on the female die after the male die was raised for 9 minutes under an environment where a hot wind of 166 C. is blowing. Like the conditions of the punching blades in the punching process, these conditions were specified based on the conditions where the white streaks are easily produced.

(53) The section of the cut piece subjected to the heat-curving process with the protective films was observed, to estimate whether the wrinkles, white cloudiness, and flames, on the protective films, occurred. The specific methods to estimate them are explained below. The results of them are summarized in Tables 2 and 4.

(54) The protective films of the cut piece subjected to the heat-curving process were removed. Then it was transferred onto the mold cavity for injection molding. Then the aromatic polycarbonate composition (containing an ultraviolet absorber) was injected. The conditions of the injection molding process were 310 C. for the temperature of the resin, 125 MPa for the pressure of the injection, 80 C. for the temperature of the mold, and 70 seconds for the injection molding cycle.

(55) The results of the observation of the white streaks are summarized in Tables 2 and 4.

(56) Shape of the Cut Piece

(57) The shape of the punched piece of the functional sheet with the protective films is a vertical section, such as a slit shape, a capsule, or a straw rice bag, where both sides of the line that passes through the center of a disc, whose diameter is 80 mm, are cut perpendicularly in the same width, 55 mm. Both sides that are not parallel have small projections on an arc of each side. The projections are used for positioning [in a mold for heat-curving process]. The long direction of the cut piece is parallel to the direction of the absorption axis of the polarizing film.

(58) The Resin for Injection Molding

(59) An aromatic polycarbonate resin (viscosity-average molecular weight: 23,000; Trade name: Iupiron CLS3400; Mitsubishi Engineering-Plastics Co. Ltd.)

(60) Mold for Injection Molding

(61) Plano lenses for no power eye-glasses: the molding cavity is a partial spherical body that has diameter that is 80 mm and about 8R. It includes an insert sheet that is corrected for an aberration and is 2 mm thick. On the opposite side of the gate of the cavity, there are projecting parts with a through hole that is used in the finishing processes for making sunglasses. The functional sheet is set on the concave surface of the mold cavity. The cavity has a projection that receives the projecting part for positioning the cut piece so that the straight parts of the slit or the straw rice bag orthogonally cross with the direction from the gate to the opposite side.

(62) Thus, when molten resin is inserted, it is spread and moves from the gate along the partial sphere and in the concave surface, the resin hits the straight parts of the cut piece and moves over the cut piece and reaches the projecting parts located on the opposite side of the gate while gradually shrinking.

(63) Melting Point

(64) The melting point is measured by using DSC (differential scanning calorimetry). The rate of the temperature increase is 10 C./min. The weight of a sample is 10 mg.

(65) Observation of the Section

(66) On the section of the cut and heated curved piece, a part of the protective film on the cut section was observed as a projecting and falling part. The part adhered to the cut section of the functional sheet. This observation was carried out by using an optical microscope. The length of the projecting and falling part of the protective film was measured by subtracting the thickness of the protective film.

(67) Occurrence of White Streaks

(68) The presence of the white streaks is observed by visual inspection. The white streaks are seen as growing white lines from the end of the cut surface along with the direction of the flow of the injected resin and in between the cut piece and injected resins. Most of the white streaks are 1-2 cm long. In this example, several millimeters of white lines are also defined as white streaks.

(69) Occurrence of the wrinkles produced by the separation of the adhesive layer of the protective films and the surface of the functional sheet

(70) The wrinkles of the heat-curving products were produced by the separation of the adhesive layer of the protective films and the surface of the functional sheet. They were 5-10 mm long. The estimation of the wrinkles were carried out by visual inspection.

(71) Exfoliation of the Protective Films

(72) The exfoliation of the protective films from the functional sheet after the heat-curving process was estimated as to whether the film could be manually peeled off.

(73) Unevenness

(74) The unevenness is seen as shape changes on the surface of the protective film on the heat-curved functional sheets. The depth of the concave parts of the shape changes were about 20-100 m. About 100-600 m of the length or width of the concave parts were observed by visual inspection by using the light of a fluorescent lamp reflected from the surface of the sample.

(75) Flames

(76) The flames were seen as changes on the shape of the surface of the protective film of the heat-curved products. They were observed by visual inspection where a sample is placed between a fluorescent lamp and the eyes of an observer.

(77) TABLE-US-00001 TABLE 1 Comparative Comparative Comparative Comparative Example 1 Example 2 Example 1 Example 2 Example 3 Example 4 Method for Coextrusion Coextrusion Stacked Coextrusion Coextrusion Coextrusion producing the product protective film of two sheets Total thickness 70 70 90 70 50 70 (m) Adhesive Type PPSM1 PPSM1 PE1 PE2 PE2 PPSM2 layer of resin thickness 20 20 50 20 20 20 (m) Base Type PP1 PP1 PP1 PP1 PP1 PP1 layer of resin thickness 30 30 40 30 30 30 (m) Support Type PP2 layer of resin thickness 20 (m) Melting Adhesive 138 142 125 88 128 128 point layer ( C.) Base 165 163 166 163 163 165 layer Support 142 layer Notes: PPSM1: a composition of a low-density polypropylene that has a melting point of about 140 C. and a SEBE elastomer. *SEBS elastomer: styrene-ethylene-butene-styrene copolymer PPSM2: a composition of a low-density polypropylene that has a melting point of about about 130 C. and a SEBE elastomer. PP1: a low-density polypropylene that has a melting point of about 160 C. PP2: a low-density polypropylene that has a melting point of about 140 C. PE1: a high-density polypropylene that has a melting point of about 120 C. PE2: a low-density polypropylene that has a melting point of about 90 C.

(78) TABLE-US-00002 TABLE 2 Comparative Comparative Comparative Comparative Example 1 Example 2 Example 1 Example 2 Example 3 Example 4 Projecting Size 136 168 503 322 382 94 and (m) falling part Exfoliation X X White Yes/No No No Yes Yes Yes No streaks Incidence 0 0 93.6 88.3 86.0 0 (%) Note: Exfoliation: The protective films were smoothly peeled off. ExfoliationX: The protective films could not be peeled off.

(79) TABLE-US-00003 TABLE 3 Comparative Comparative Example 3 Example 4 Example 5 Example 5 Example 6 Method for Coextrusion Coextrusion Coextrusion Stacked Coextrusion producing the product of protective film two sheets Total thickness 74 71 70 90 67 (m) Adhesive Type of PPSM PPSM PPSM PE1 PPSM layer resin thickness 22 21 19 50 18 (m) Base Type of PP1 PP1 PP1 PP1 PP1 layer resin thickness 18 22 21 40 49 (m) Middle Type of PP2 PP4 PP3 layer resin thickness 34 28 30 (m) Melting Adhesive 139 141 140 125 142 point layer C. Base 160 161 162 165 163 layer Middle 142 120 131 layer Notes: PPSM: a composition of a low-density polypropylene that has a melting point of about 140 C. and a SEBE elastomer. *SEBS elastomer: styrene-ethylene-butene-styrene copolymer PP1: a low-density polypropylene that has a melting point of about 160 C. PP2: a low-density polypropylene that has a melting point of about 140 C. PP3: a low-density polypropylene that has a melting point of about 130 C. PP4: a low-density polypropylene that has a melting point of about 120 C. PE1: a high-density polyethylene that has a melting point of about 120 C.

(80) TABLE-US-00004 TABLE 4 Comparative Comparative Example 3 Example 4 Example 5 Example 5 Example 6 Wrinkles X X X Exfoliation X X Flames X X Unevenness X X White Incidence 0 0 0 98 0 streaks (%) White X X cloudiness Notes: White streaks: No white streak in the lens. White streaksX: White streaks several millimeters or more long were observed. Wrinkles: No wrinkle on the surface of the protective film WrinklesX: Wrinkles on the surface of the protective film were observed. Exfoliation: The protective films are smoothly peeled off. ExfoliationX: The protective films cannot be peeled off. Unevenness: No unevenness on the functional film after the protective films were peeled off. UnevennessX: Unevenness on the functional film after the protective films were peeled off was observed. White cloudiness: No white cloudiness in the injection molded lens White cloudinessX: White cloudiness in the injection molded lens was observed.

INDUSTRIAL APPLICABILITY

(81) The present invention provides a functional sheet with the protective films. By using this functional sheet, aromatic polycarbonate injection molded lenses that show reduced defects derived from the conditions of the steps of processing the sheet, such as white streaks, wrinkles of the protective film derived from the exfoliation between the adhesive layer and the surface of the functional sheet, and the unevenness of the protective film, can be provided.